Ditron Dental MPI-11600Recalls & reported problems
Ditron Dental Ltd · Molecular Precision Implant Ø6.0mm L11.5mm · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 07290109280301), received between Apr 17, 2024 and Jul 30, 2025 — classified as 10 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (9 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate9
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Inadequate Osseointegration8
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Infection1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryApr 17, 2024Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19123882 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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